Fabry disease: Four case reports of meningioma and a review of the literature on other malignancies

Fabry disease (FD) is an X-linked lysosomal storage disorder caused by loss of function mutations in the GLA gene at Xq22 with subsequent functional deficiency of alpha-galactosidase A, resulting in the accumulation of globotriaosylceramide (GL-3 or Gb3) in multiple cells types throughout the body....

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Bibliographic Details
Main Authors: Beth L. Thurberg, MD, PhD, Dominique P. Germain, MD, PhD, Fernando Perretta, MD, Iulia E. Jurca-Simina, MD, Juan M. Politei, MD
Format: Article
Language:English
Published: Elsevier 2017-06-01
Series:Molecular Genetics and Metabolism Reports
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2214426916300866